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2-thioxo-1,2,5,6,7,8,9,10,11,12-decahydrocyclodeca[b]pyridine-3-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

154384-03-9

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154384-03-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 154384-03-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,3,8 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 154384-03:
(8*1)+(7*5)+(6*4)+(5*3)+(4*8)+(3*4)+(2*0)+(1*3)=129
129 % 10 = 9
So 154384-03-9 is a valid CAS Registry Number.

154384-03-9Upstream product

154384-03-9Downstream Products

154384-03-9Relevant academic research and scientific papers

A convenient synthesis of 5-deaza nonclassical antifolates: Reaction of cyanothioacetamide with sodium salts of 2-(hydroxymethylene)-1-cycloalkanones

Elgemeie, Galal E. H.,Hussain, Badria A. W.

, p. 199 - 204 (1994)

Condensation of cyanothioacetamide with sodium salts of 2-(hydroxymethylene)-1-cycloalkanones afforded the corresponding pyridine-2(1H)-thiones 4. Compounds 4 served as a key intermediate for the synthesis of condensed 2,4-diaminopyrido[2,3-d]pyridines 7. Compounds 7 were of interest as potential inhibitors of dihydrofolate reductase.

Synthesis and antiproliferative activity of 2-chlorophenyl carboxamide thienopyridines

van Rensburg, Michelle,Leung, Euphemia,Haverkate, Natalie A.,Eurtivong, Chatchakorn,Pilkington, Lisa I.,Reynisson, Jóhannes,Barker, David

supporting information, p. 135 - 138 (2016/12/27)

3-Amino-2-arylcarboxamide-thieno[2,3-b]pyridines are a known class of antiproliferative compounds with activity against the phospholipase C enzyme. To further investigate the structure activity relationships of these derivatives a series of analogues were prepared modifying key functional groups. It was determined that modification of the 3-amino and 2-aryl carboxamide functionalities resulted in complete elimination of activity, whilst modification at C-5 allowed compounds of greater activity to be prepared.

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